BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

276 related articles for article (PubMed ID: 20664694)

  • 1. A novel PAX6 mutation in a large Chinese family with aniridia and congenital cataract.
    Cai F; Zhu J; Chen W; Ke T; Wang F; Tu X; Zhang Y; Jin R; Wu X
    Mol Vis; 2010 Jun; 16():1141-5. PubMed ID: 20664694
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Mutation analysis of paired box 6 gene in inherited aniridia in northern China.
    Chen P; Zang X; Sun D; Wang Y; Wang Y; Zhao X; Zhang M; Xie L
    Mol Vis; 2013; 19():1169-77. PubMed ID: 23734086
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A recurrent PAX6 mutation is associated with aniridia and congenital progressive cataract in a Chinese family.
    Jin C; Wang Q; Li J; Zhu Y; Shentu X; Yao K
    Mol Vis; 2012; 18():465-70. PubMed ID: 22393272
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Identification of dominant FOXE3 and PAX6 mutations in patients with congenital cataract and aniridia.
    Brémond-Gignac D; Bitoun P; Reis LM; Copin H; Murray JC; Semina EV
    Mol Vis; 2010 Aug; 16():1705-11. PubMed ID: 20806047
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A novel PAX6 deletion in a Chinese family with congenital aniridia.
    Chen JH; Lin W; Sun G; Huang C; Huang Y; Chen H; Pang CP; Zhang M
    Mol Vis; 2012; 18():989-95. PubMed ID: 22550392
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A novel PAX6 gene mutation in a Chinese family with aniridia.
    Song S; Liu Y; Guo S; Zhang L; Zhang X; Wang S; Lu A; Li L
    Mol Vis; 2005 May; 11():335-7. PubMed ID: 15889018
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Mutation analysis of the PAX6 gene in a family with congenital aniridia and cataract].
    Lin Y; Li J; Yang Y; Yang JY; Zhang B; Tang X; Liu XQ; Lu F; Yang ZL
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Oct; 26(5):542-5. PubMed ID: 19806578
    [TBL] [Abstract][Full Text] [Related]  

  • 8. PAX6 analysis of one family and one sporadic patient from southern China with classic aniridia.
    Lin Y; Liu X; Liang X; Li B; Jiang S; Ye S; Yang H; Lou B; Liu Y
    Mol Vis; 2011; 17():3116-20. PubMed ID: 22171157
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Molecular genetics of familial nystagmus complicated with cataract and iris anomalies.
    Yan N; Zhao Y; Wang Y; Xie A; Huang H; Yu W; Liu X; Cai SP
    Mol Vis; 2011; 17():2612-7. PubMed ID: 22025896
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A novel PAX6 mutation in Chinese patients with severe congenital aniridia.
    He Y; Pan Z; Luo F
    Curr Eye Res; 2012 Oct; 37(10):879-83. PubMed ID: 22621390
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Mutation analysis of PAX6 in a Chinese family and a patient with a presumed sporadic case of congenital aniridia.
    Luo F; Zhou L; Ma X; He Y; Zou L; Jie Y; Liu J; Pan Z
    Ophthalmic Res; 2012; 47(1):27-31. PubMed ID: 21691140
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Three new PAX6 mutations including one causing an unusual ophthalmic phenotype associated with neurodevelopmental abnormalities.
    Dansault A; David G; Schwartz C; Jaliffa C; Vieira V; de la Houssaye G; Bigot K; Catin F; Tattu L; Chopin C; Halimi P; Roche O; Van Regemorter N; Munier F; Schorderet D; Dufier JL; Marsac C; Ricquier D; Menasche M; Penfornis A; Abitbol M
    Mol Vis; 2007 Apr; 13():511-23. PubMed ID: 17417613
    [TBL] [Abstract][Full Text] [Related]  

  • 13. PAX6 analysis of two sporadic patients from southern China with classic aniridia.
    Lin Y; Liu X; Yu S; Luo L; Liang X; Wang Z; Chen C; Zhu Y; Ye S; Yan H; Liu Y
    Mol Vis; 2012; 18():2190-4. PubMed ID: 22919266
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Identification of novel mutant PAX6 alleles in Indian cases of familial aniridia.
    Neethirajan G; Nallathambi J; Krishnadas SR; Vijayalakshmi P; Shashikanth S; Collinson JM; Sundaresan P
    BMC Ophthalmol; 2006 Jun; 6():28. PubMed ID: 16803629
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [A novel mutation of the PAX6 gene identified in a northeastern Chinese family with congenital aniridia].
    Kang Y; Yuan HP; Li YY
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2008 Apr; 25(2):172-5. PubMed ID: 18393239
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A novel PAX6 deletion in a Chinese family with congenital aniridia.
    Liu Q; Wan W; Liu Y; Liu Y; Hu Z; Guo H; Xia K; Jin X
    Gene; 2015 May; 563(1):41-4. PubMed ID: 25746674
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [A novel mutation of the PAX6 gene in a Chinese family with aniridia].
    Kang Y; Yuan HP; Li X; Li QJ; Wu Q; Hu Q
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2010 Aug; 27(4):376-80. PubMed ID: 20677140
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A novel mutation of PAX6 identified in a Chinese twin family with congenital aniridia complicated with nystagmus.
    Cao X; Zhou XM; Gan R; Jiang LQ; Lu L; Wang Y; Fan N; Yin Y; Yan NH; Yu WH; Liu XY
    Genet Mol Res; 2014 Oct; 13(4):8679-85. PubMed ID: 25366758
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Two novel PAX6 mutations identified in northeastern Chinese patients with aniridia.
    Yuan H; Kang Y; Shao Z; Li Y; Yang G; Xu N
    Mol Vis; 2007 Aug; 13():1555-61. PubMed ID: 17893655
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Identification of a novel PAX6 mutation in a family with congenital aniridia].
    Li J; Zhao L; Cai XJ; Lu L; Li G
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2013 Oct; 30(5):579-81. PubMed ID: 24078574
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 14.